Literature DB >> 12818952

Isoflurane depresses diffuse noxious inhibitory controls in rats between 0.8 and 1.2 minimum alveolar anesthetic concentration.

Steven L Jinks1, Joseph F Antognini, Earl Carstens.   

Abstract

UNLABELLED: Diffuse noxious inhibitory control (DNIC) occurs when the response to a noxious stimulus is inhibited by a second, spatially remote noxious stimulus. The minimum alveolar anesthetic concentration (MAC) to suppress movement is not altered by a second remote noxious stimulus. We hypothesized that DNIC would be depressed in the peri-MAC range. Rats were anesthetized with isoflurane, and MAC was measured. We recorded dorsal horn neuronal responses to noxious thermal stimulation of the hindpaw, with or without concomitant supramaximal noxious mechanical stimulation of the tail or contralateral hindpaw. At 0.8 MAC, the tail clamp decreased neuronal responses 70% compared with control heat-evoked responses (from 1032 +/- 178 impulses per minute to 301 +/- 135 impulses per minute; P < 0.05). The tail clamp had no significant effect on neuronal responses at 1.2 MAC (from 879 +/- 139 impulses per minute to 825 +/- 191 impulses per minute; P > 0.05). Similarly, 1.2 MAC isoflurane significantly depressed DNIC elicited by hindpaw clamping. In another group, the cervical spinal cord was reversibly blocked by cooling to determine whether the inhibition was mediated supraspinally. With spinal cord cooling, the counterstimulus-evoked inhibition was not observed at 0.8 MAC. These results suggest that DNIC involves supraspinal structures and is present at sub-MAC isoflurane concentrations but is depressed at more than 1 MAC. IMPLICATIONS: Diffuse noxious inhibitory control (DNIC) occurs when a noxious stimulus is perceived as being less painful when a second noxious stimulus is applied elsewhere on the body. DNIC is present in anesthetized animals, although how anesthesia affects it is unknown. We found that isoflurane depressed DNIC in the transition from 0.8 to 1.2 minimum alveolar anesthetic concentration, suggesting that DNIC is depressed in the anesthetic range needed to suppress movement.

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Year:  2003        PMID: 12818952     DOI: 10.1213/01.ane.0000066259.39584.f7

Source DB:  PubMed          Journal:  Anesth Analg        ISSN: 0003-2999            Impact factor:   5.108


  6 in total

1.  Volatile anesthetic effects on midbrain-elicited locomotion suggest that the locomotor network in the ventral spinal cord is the primary site for immobility.

Authors:  Steven L Jinks; Milo Bravo; Shawn G Hayes
Journal:  Anesthesiology       Date:  2008-06       Impact factor: 7.892

2.  Rat dorsal horn nociceptive-specific neurons are more sensitive than wide dynamic range neurons to depression by immobilizing doses of volatile anesthetics: an effect partially reversed by the opioid receptor antagonist naloxone.

Authors:  Linda S Barter; Earl E Carstens; Steven L Jinks; Joseph F Antognini
Journal:  Anesth Analg       Date:  2009-08       Impact factor: 5.108

3.  Neurons in the ventral spinal cord are more depressed by isoflurane, halothane, and propofol than are neurons in the dorsal spinal cord.

Authors:  JongBun Kim; Aubrey Yao; Richard Atherley; Earl Carstens; Steven L Jinks; Joseph F Antognini
Journal:  Anesth Analg       Date:  2007-10       Impact factor: 5.108

4.  Brainstem regions affecting minimum alveolar concentration and movement pattern during isoflurane anesthesia.

Authors:  Steven L Jinks; Milo Bravo; Omar Satter; Yuet-Ming Chan
Journal:  Anesthesiology       Date:  2010-02       Impact factor: 7.892

5.  Suppression of the descending inhibitory pathway by continuous thoracic intrathecal lidocaine infusion reduces the thermal threshold of the tail-flick response in rats.

Authors:  Yoshihiro Takasugi; Tatsushige Iwamoto; Masaki Fuyuta; Yoshihisa Koga; Masaki Tabuchi; Hideaki Higashino
Journal:  J Anesth       Date:  2009-08-14       Impact factor: 2.078

6.  Involvement of spinal α2 -adrenoceptors in prolonged modulation of hind limb withdrawal reflexes following acute noxious stimulation in the anaesthetized rabbit.

Authors:  John Harris
Journal:  Eur J Neurosci       Date:  2016-02-28       Impact factor: 3.386

  6 in total

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